Evidence map›Paper›PMID 42631092›Full record

ArticleACS nanoscience Au2026

High-Throughput SWCNT NIR-II Spectroscopy Enables Cell and In Vivo Applications.

Atara R Israel, Zachary Cohen, Nazifa Rahman, Anastasiia Vasylaki, Amelia K Ryan, Syeda Rahman, Pratyusha Ghosh, Ryan M Williams

Abstract read
In one paragraph

Article in ACS nanoscience Au, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Atara R IsraelThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Zachary CohenThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Nazifa RahmanThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Anastasiia VasylakiThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Amelia K RyanThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Syeda RahmanThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Pratyusha GhoshThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.
Ryan M WilliamsThe City College of New York, Department of Biomedical Engineering, New York, New York 10031, United States.ORCID https://orcid.org/0000-0002-2381-8732

Funding

G-RISE: Graduate Research Initiative for Student Advancement at The City College of New YorkT32GM136499 · NIGMS · CITY COLLEGE OF NEW YORK · PI RUTH E. STARK · 2020 to 2026
$4.9M
Integrating Real-Time Multi-System Cytokine Signaling in Chronic DiseaseR35GM142833 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI WILLIAMS, RYAN MARTIN · 2021 to 2025
$2.4M
NIGMS NIH HHS R35 GM142833NIGMS NIH HHS T32 GM136499
6 · The paper itself

Abstract

Diagnostic sensor development and clinical translation lag, in part, due to a lack of rapid, high-throughput screening methodologies. Optimization of high-throughput sensor development and deployment will likely help in expediting tools toward the clinic. To address this issue, we optimized high-throughput screening parameters using a near-infrared (NIR-II) plate reader attached to an external probe for in vivo testing. We assessed spectroscopy parameters to improve the speed and precision in screening a single-walled carbon nanotube (SWCNT)-based optical sensor. To do so, we assessed the appropriate well-plate specifications, including laser power, excitation wavelength, exposure time, and focal height parameters for SWCNT-based optical sensor development. We also used the plate reader to screen fluorescent SWCNTs that were endocytosed by a macrophage cell line. We then performed NIR probe spectroscopy to assess SWCNTs embedded within a methylcellulose hydrogel. Finally, we used the NIR probe to measure the SWCNT center wavelength and intensity from live immunocompetent mice. We anticipate that this framework may be broadly applicable to the development of near-infrared nanosensors with the potential for more rapid clinical diagnostic translation.

Indexed as

bionanosensorin vivomacrophagesnear-infrared (NIR) fluorescenceNIR-II short-wave infrared (SWIR)SWCNT

Identifiers

PMID42631092
PMCPMC13495494

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.